(S)-1-cyano-1,2,3,4-tetrahydronaphthalen-1-yl (R)-2-methoxy-2-phenylacetate

Base Information

Chemical Name:(S)-1-cyano-1,2,3,4-tetrahydronaphthalen-1-yl (R)-2-methoxy-2-phenylacetate
CAS No.:1092080-99-3
Molecular Formula:C₂₀H₁₉NO₃
Molecular Weight:321.376
Hs Code.:

Synonyms:(S)-1-cyano-1,2,3,4-tetrahydronaphthalen-1-yl (R)-2-methoxy-2-phenylacetate

Suppliers and Price of (S)-1-cyano-1,2,3,4-tetrahydronaphthalen-1-yl (R)-2-methoxy-2-phenylacetate

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (S)-1-cyano-1,2,3,4-tetrahydronaphthalen-1-yl (R)-2-methoxy-2-phenylacetate

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Technology Process of (S)-1-cyano-1,2,3,4-tetrahydronaphthalen-1-yl (R)-2-methoxy-2-phenylacetate

There total 2 articles about (S)-1-cyano-1,2,3,4-tetrahydronaphthalen-1-yl (R)-2-methoxy-2-phenylacetate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 80.0%

: 1092080-61-9
(S)-1-hydroxy-1,2,3,4-tetrahydronaphthalene carbonitrile

: 3966-32-3
(R)-methoxyphenylacetic acid

: 1092080-99-3
(S)-1-cyano-1,2,3,4-tetrahydronaphthalen-1-yl (R)-2-methoxy-2-phenylacetate

Guidance literature:: With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; Inert atmosphere;
DOI:10.1002/ejoc.201001107

Reference yield:

: 3966-32-3
(R)-methoxyphenylacetic acid

: 76311-47-2
(+/-)-1-hydroxy-1,2,3,4-tetrahydronaphthalene carbonitrile

: 1092080-99-3
(S)-1-cyano-1,2,3,4-tetrahydronaphthalen-1-yl (R)-2-methoxy-2-phenylacetate

Guidance literature:: With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; Inert atmosphere;
DOI:10.1021/ol8023314